Skip to main content
Search
Explore journals
Get published
About BMC
My account
Search all BMC articles
Search
Orphanet Journal of Rare Diseases
Home
About
Articles
Submission Guidelines
Table 3
Genetic heterogeneity expressed as the number of mutations per examined gene in 124 NCL patients
From:
Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy
GENE
Patients
Alleles
Mutations
CLN1
17
34
11
CLN2
29
56
17
CLN3
16
32
3
CLN5
7
14
7
CLN6
21
42
17
CLN7
14
28
14
CLN8
7
14
7
CLN10
1
2
1
Back to article page